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Urea cycle disorders: a life-threatening yet treatable cause of metabolic encephalopathy in adults.
Blair, Nicholas F; Cremer, Philip D; Tchan, Michel C.
Afiliação
  • Blair NF; Department of Neurology, Royal North Shore Hospital, Sydney, Australia.
  • Cremer PD; Department of Neurology, Royal North Shore Hospital, Sydney, Australia.
  • Tchan MC; Adult Genetic Metabolic Disorders Service, Westmead Hospital, Sydney, Australia.
Pract Neurol ; 15(1): 45-8, 2015 Feb.
Article em En | MEDLINE | ID: mdl-25125564
Urea cycle disorders are inborn errors of metabolism that, in rare cases, can present for the first time in adulthood. We report a perplexing presentation in a woman 4 days postpartum of bizarre and out-of-character behaviour interspersed with periods of complete normality. Without any focal neurological signs or abnormality on initial investigations, the diagnosis became clear with the finding of a significantly elevated plasma ammonia level, just as she began to deteriorate rapidly. She improved following intravenous dextrose and lipid emulsion, together with sodium benzoate, arginine and a protein-restricted diet. She remains well 12 months later with no permanent sequelae. Whilst this is a rare presentation of an uncommon disease, it is a treatable disorder and its early diagnosis can prevent a fatal outcome.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encefalopatias Metabólicas / Distúrbios Congênitos do Ciclo da Ureia Tipo de estudo: Screening_studies Limite: Adult / Female / Humans Idioma: En Revista: Pract Neurol Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encefalopatias Metabólicas / Distúrbios Congênitos do Ciclo da Ureia Tipo de estudo: Screening_studies Limite: Adult / Female / Humans Idioma: En Revista: Pract Neurol Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Austrália